Very distantly similar to animal TMEM8 and MMD2 proteins. Its function is obscure, although gene fusions with lipid hydrolases suggest a related function
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 20 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 22 |
GO:0016020 | membrane | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
Related structures:
AlphaFold database: Q4QEJ7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.299 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.328 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.439 |
DEG_SCF_FBW7_1 | 196 | 203 | PF00400 | 0.557 |
DOC_CKS1_1 | 197 | 202 | PF01111 | 0.563 |
DOC_MAPK_DCC_7 | 118 | 126 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 118 | 127 | PF00069 | 0.363 |
DOC_PP4_FxxP_1 | 89 | 92 | PF00568 | 0.512 |
DOC_SPAK_OSR1_1 | 118 | 122 | PF12202 | 0.343 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.540 |
LIG_14-3-3_CanoR_1 | 118 | 122 | PF00244 | 0.335 |
LIG_BRCT_BRCA1_1 | 188 | 192 | PF00533 | 0.380 |
LIG_BRCT_BRCA1_1 | 40 | 44 | PF00533 | 0.421 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.342 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.341 |
LIG_IBAR_NPY_1 | 91 | 93 | PF08397 | 0.428 |
LIG_Integrin_RGD_1 | 216 | 218 | PF01839 | 0.451 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.260 |
LIG_LIR_LC3C_4 | 106 | 109 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 41 | 45 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.255 |
LIG_MLH1_MIPbox_1 | 188 | 192 | PF16413 | 0.380 |
LIG_PDZ_Class_1 | 216 | 221 | PF00595 | 0.623 |
LIG_Pex14_1 | 115 | 119 | PF04695 | 0.267 |
LIG_Pex14_2 | 101 | 105 | PF04695 | 0.345 |
LIG_Pex14_2 | 126 | 130 | PF04695 | 0.284 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.408 |
LIG_Pex14_2 | 44 | 48 | PF04695 | 0.466 |
LIG_REV1ctd_RIR_1 | 25 | 36 | PF16727 | 0.394 |
LIG_SH2_PTP2 | 83 | 86 | PF00017 | 0.328 |
LIG_SH2_PTP2 | 93 | 96 | PF00017 | 0.467 |
LIG_SH2_SRC | 93 | 96 | PF00017 | 0.381 |
LIG_SH2_STAT3 | 206 | 209 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.469 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.372 |
LIG_SUMO_SIM_anti_2 | 17 | 24 | PF11976 | 0.342 |
LIG_TRFH_1 | 127 | 131 | PF08558 | 0.464 |
LIG_TYR_ITIM | 81 | 86 | PF00017 | 0.462 |
LIG_UBA3_1 | 103 | 112 | PF00899 | 0.359 |
LIG_UBA3_1 | 125 | 134 | PF00899 | 0.415 |
LIG_UBA3_1 | 162 | 170 | PF00899 | 0.378 |
LIG_WRC_WIRS_1 | 188 | 193 | PF05994 | 0.391 |
LIG_WRC_WIRS_1 | 45 | 50 | PF05994 | 0.357 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.291 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.259 |
MOD_GlcNHglycan | 5 | 9 | PF01048 | 0.458 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.323 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.508 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.330 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.377 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.443 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.320 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.312 |
MOD_NEK2_2 | 187 | 192 | PF00069 | 0.367 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.372 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.304 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.286 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.328 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.279 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.414 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.537 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.469 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.499 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1L8 | Leptomonas seymouri | 34% | 98% |
A0A0N1IHQ2 | Leptomonas seymouri | 56% | 100% |
A0A0S4J3W8 | Bodo saltans | 40% | 98% |
A0A0S4J4A1 | Bodo saltans | 42% | 100% |
A0A1X0NUH8 | Trypanosomatidae | 38% | 100% |
A0A1X0NUR6 | Trypanosomatidae | 45% | 100% |
A0A3Q8ICP7 | Leishmania donovani | 94% | 100% |
A0A3R7NKX5 | Trypanosoma rangeli | 44% | 100% |
A0A3S5H6Z5 | Leishmania donovani | 33% | 98% |
A4H8U8 | Leishmania braziliensis | 71% | 100% |
A4HX66 | Leishmania infantum | 94% | 100% |
A4HX67 | Leishmania infantum | 33% | 98% |
C9ZTT2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZTT4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZTT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9ARC3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9ARC4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 98% |
Q4QEJ6 | Leishmania major | 34% | 100% |
V5ASR1 | Trypanosoma cruzi | 43% | 100% |
V5BCQ2 | Trypanosoma cruzi | 37% | 100% |